专利摘要:
SUMMARY Modular anode assemblies (200) are used in electrolytic oxide reduction systems for scalable production of reduced metal via electrolysis. Assembly includes a channel frame (201) connected to a plurality of anode rods (210) extending into an electrolyte. An electrical system (280, 285, 286) drives the rods because it is isolated from the channel frame. A cooling system (240, 245) removes heat from the anode rods and the electrical system. An anode guard attaches to the duct frame to avoid accidental electric shock or damage during handling or repositioning. Each anode rod can be divided into upper and lower sections to allow easy repair and replacement of lower sections. The modular assemblies may have standardized components to allow placement at multiple points within a reducing system by positioning the modular anode assemblies in the reduction system and applying electrical power to the multiple anode assemblies.
公开号:SE537832C2
申请号:SE1350853
申请日:2011-09-29
公开日:2015-10-27
发明作者:James L Willit;Laurel A Barnes;Stanley G Wiedmeyer;Mark A Williamson
申请人:Ge Hitachi Nucl Energy America;
IPC主号:
专利说明:

[1] [0001] This invention is challenged with state standing under contract number DE-ACO2-06CH11357, issued by U.S. Pat. Department of Energy. The state has certain rights to the invention.
[2] One- and multi-stage electrochemical processes are useful for reducing metal oxides to their corresponding metallic (unoxidized) state. Conventionally, such processes are used to recover hogren metal, metals from a contaminated feed, and / or to extract metals from their metal oxide ores.
[3] Multistage processes conventionally dissolve metal or ore into an electrolyte followed by an electrochemical probing or selective electrotransport step to recover unoxidized metal. For example, in the recovery of uranium from spent carbon monoxide fuel, a chemical reduction of the uranium oxide at 650 ° C is carried out by a reducing agent such as Li dissolved in narrow LiCl, to produce uranium and Li 2 O. The solution was then subjected to electro-extraction, used in lost Li 2 O in the narrow LiCl1 to be electrolytically degraded to regenerate Li. The uranium metal is produced for further use, such as nuclear fuel in commercial nuclear reactors.
[4] One-step processes generally sink a metal oxide into molten electrolyte, selected to be compatible with the metal oxide, along with a cathode and anode. The cathode is in electrical contact with the metal oxide and, by charging the anode and the cathode (and the metal oxide via the cathode), the metal oxide is reduced via electrolytic conversion and ion exchange through the narrow electrolyte.
[5] One-step processes generally use Mire components and / or steps in the handling and movement of molten salts and metals, limit the amount of free-flowing or excess reduction metal, have improved process control and are compatible with a variety of metal oxides in different starting states / mixtures with higher purity results. compared to multi-step processes.
[6] Exemplary embodiments include modular anode assemblies and electrolytic oxide reduction systems using such modular assemblies. Each unit may comprise a channel frame connected to several anode rods extending into an electrolyte in a reduction system. The rods can be driven by an electrical system which, with the rods, is insulated from the channel frame. The electrical system comprises an anode block into which the anode rod is located and is electrically connected, and a busbar providing electrical power to the anode block. The electrical systems can be resilient at high operating temperatures by including a sliding contact that allows thermal expansion without damage. A cooling system removes heat from the anode rod and the electrical system by, for example, blowing an active, inert cooling gas onto the components. An anode cover can be attached to the duct frame to avoid accidental electric shock or damage to unit components during handling and repositioning of the modular units. Each anode rod can be divided into upper and lower sections to allow easy repair and replacement of older sections that are in contact with a potentially corrosive electrolyte. The modular units may have standardized electrical and gas-cold / drain connectors to allow placement at multiple points within a reducing system.
[7] Exemplary methods can drive an electrolytic oxide reduction system by positioning the modular anode assemblies in the reduction system and providing electrical power to the multiple anode assemblies through the electrical system in the assemblies to charge the anode rods. Since the anode rods extend into an electrolyte which is in contact with the target oxide and cathode, the metal oxide can be reduced to its metallic form. The electrolyte may be fluidized by melting or dissolving so that the anode rod in each of the modular anode rod assemblies may extend into the electrolyte. The cooling system can be operated during the provision of power to remove heat from the anode rod and the electrical system when it is connected to a gas source and a gas drain via the cooling system.
[8] FIG. 1 is an illustration of an exemplary embodiment of an electrolytic oxide reduction system.
[9] FIG. 2 is another illustration of the exemplary embodiment of the oxide reduction system of FIG. 1 in an alternative embodiment. 3
[10] FIG. 3 is an illustration of an exemplary embodiment of anode assembly usable in an exemplary embodiment system.
[11] FIG. 4 is an illustration of another exemplary embodiment of anode assembly without an anode cover.
[12] Exemplary embodiments will hereinafter be described in detail with reference to the accompanying drawings. Specific structural and functional details described herein are, however, only representative for the purpose of describing exemplary embodiments. The exemplary embodiments may be embodied in many alternative forms and should not be construed as limited to exemplary embodiments only.
[13] It will be appreciated that, although the terms first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are used only to distinguish one element from another. For example, a first element may be termed a second element, and on the same salt, a second element may be termed a first element, without departing from the scope of exemplary embodiments. As used herein, the term "and / or" includes any and all combinations of one or more of the associated parts indicated.
[14] It will be appreciated that when one element is referred to as being "connected", "connected", "paired", "attached", or "fixed" to another element, it may be directly connected or connected to the other. element 4 or intermediate elements may be present. In contrast, when one element is referred to as being "directly connected" or "directly connected" to another element, there are no intermediate elements present. Other words used to describe the relationship between elements should be interpreted in a similar way (eg "between" versus "directly between", "adjacent" versus "directly adjacent", etc.).
[15] As used herein, the singular forms "en" and "den" are intended to include the plural forms unless the language explicitly indicates otherwise. It is further understood that the terms "including", "including", "including" and / or "inclusive", when used herein, specify the occurrence of specified features, units, steps, operations, elements and / or components, but do not exclude the occurrence or addition of one or more other features, devices, steps, operations, elements, components and / or groups ddrav.
[16] It should also be noted that in some alternative implementations, the listed functions / actions may occur outside the order noted in the figures or described in the description. For example, two figures or steps shown in sequence can, in fact, be performed in series and simultaneously, or can sometimes be performed in reverse order or repetitively, depending on the functionality / action involved.
[17] The inventors have realized a problem in existing one-step electrolytic reduction processes in that the known processes cannot generate large amounts of reduced metallic products on a commercial or flexible scale, at least in part due to limited, static cathode size and configuration. One-step electrolytic reduction can further lack flexibility in configuration, sd as regularity of parts and possibility to replace, and in operating parameters, such as power level, operating temperature, working electrolyte etc. Exemplary systems and methods describe below dtgardar these and other problems, discussed below or not, on a unique salt.
[18] FIG. 1 is an illustration of an exemplary embodiment electrolytic oxide reduction system (EORS) 1000. Although aspects of exemplary embodiment EORS 1000 are described below and are useful with related exemplary embodiment components, the EORS 1000 is further described in the following co-pending applications: Application no. Submission Date Agent Reference. 12/977791 12/23 / 2024AR2461 (8564- 000224) 12/977839 12/23 / 2024AR246136 (8564- 000225) 12/9780012/23 / 2024AR246139 (8564- 000227) 12/978027 12/23 / 2024AR2461 (8564- 000228 ) The contents of the above-listed concurrent applications dr harmed incorporated in its entirety by male reference hari.
[19] As shown in Fig. 1, exemplary embodiment EORS 1000 comprises several modular components that allow electrolytic reduction 6 of several different types of metal oxides on a flexible or commercial scale. Exemplary Embodiment EORS 1000 includes an electrolyte container 1050 in contact with or on other salt heated by a heater 1051, if necessary to melt and / or dissolve an electrolyte in container 1050. Electrolyte container 1050 is filled with an evaporable electrolyte, such as a halide salt or salt comprising a soluble oxide that provides mobile oxide ions, selected based on the type of material to be reduced. For example, CaCl 2 and CaO, or CaF 2 and CaO, or nd_gra other Cabased electrolytes, or a lithium-based electrolyte mixture sd. such as Li C1 and Li2O, are used to reduce oxides of salt-like earth metals, or oxides of actinides such as uranium or plutonium oxides, or complex oxides such as spent nuclear fuel. The electrolyte may further be selected based on its melting point. For example, an electrolyte salt mixture of LiCl or LW and LiCl 2 may be melted at about 610 ° C at standard pressures, while a CaCl 2 and CaO mixture may require operating temperatures of about 850 ° C. Concentrations of the loose oxide moieties can be controlled during reduction by the addition of soluble oxides or chlorides by electrochemical or other means.
[20] EORS 1000 may comprise several supporting and structural parts for containing, framing, and otherwise drilling and assembling other components. For example, one or more lateral stands 1104 may extend up to and support a top plate 1108, which may include an opening (not shown) above electrolyte container 1050 to allow access thereto. Top plate 1108 may further be supported and / or insulated by a glove box (not shown) connecting to and around top plate 1108. Several standard electrical contacts 1480 (Fig. 2) and cooling coils / gas outlets may be provided on or near top plate 1108 to allow anode and cathode components to be supported by and operating through the EORS 1000 at modular positions. A lifting basket system, including a lifting boom 1105 and / or guide rods 1106 may connect and / or suspend cathode assemblies 1300 extending down into the narrow electrolyte of electrolyte container 1050. Slant lifting basket systems may allow selective lifting or other thinning of cathode assemblies 1300 without moving EORS 1000 and related components.
[21] In Fig. 1, EORS 1000 is shown with several cathode assemblies 1300 alternating with several anode assemblies 1200 supported by different standing elements and extending into electrolyte tanks 1050. The assemblies can further be driven or cooled by standardized connections to corresponding callers in EORS 1000. Also if ten cathode assemblies 1300 and eleven anode assemblies 1200 are shown in Fig. 1, any number of anode assemblies 1200 and cathode assemblies 1300 can be used in EORS 1000, depending on energy resources, amount of material to be reduced, desired amount of metal to be produced, etc. saga, individual cathode assemblies 1300 and / or anode assemblies 1200 can be added or removed to provide a flexible, and potentially large, commercial scale, electrolytic reduction system. In this way, through the modular design of exemplary embodiments EORS 1000, anode assemblies 1200 and cathode assemblies 1300, exemplary embodiments can better satisfy material production requirements and energy consumption limits in a fast, simplified one-step reduction operation. The modular design can further enable rapid repair and standardized manufacturing of exemplary embodiments, reduced manufacturing and renovation costs, and time constraints.
[22] FIG. 2 is an illustration of the EORS 1000 in an alternative configuration, with basket lifting systems including boom 1105 and guide rods 1106 raised to selectively lift only modular cathode assemblies 1300 out of electrolyte container 1050 to access, allow loading or unloading of reaction metal oxides or produced cathode assemblies. The configuration of Fig. 2 shows several modular electrical contacts 1480 aligned at modular positions around the aperture in top plate 1080. For example, electrical contacts 1480 may be knife wall contacts that allow several different orientations and positions of modular cathode assemblies 1300 and / or anode assemblies 1200 within EORS 1000.
[23] As shown in Fig. 1, a power transmission system including a bus bar 1400, anode current cable 1410, and / or cathode current cable may provide independent electrical charging to anode assemblies 1200 and / or cathode assemblies 1300, through electrical contacts (not shown). During operation, electrolyte in electrolyte container 1050 may be liquefied by heating and / or dissolving or otherwise providing a liquid electrolyte material compatible with the oxide to be reduced. Operating temperatures of the liquid electrolyte material can range from about 400-1200 ° C, based on the materials used. Oxide materials, including, for example, Nd 2 O 3, PuO 2, UO 2, complex oxides such as spent fuel or salty earth ores, etc. are loaded into cathode aggregates 9 1300, which extend into the liquid electrolyte so that the oxide material is in contact with the electrolyte and cathode aggregates.
[24] Cathode assemblies 1300 and anode assemblies 1200 are connected to power sources to provide opposite charges or polarities, and a current controlled electrochemical process takes place so that a desired electrochemically generated reduction potential is achieved at the cathode by reduction electrons flowing into the metal oxide at the cathode. Due to the generated reducing potential, oxygen freezes in the oxide material within the cathode assemblies 1300 and dissolves in the liquid electrolyte as an oxide ion. The reduced metal in the oxide material remains in the cathode assemblies 1300. The electrolytic reaction at the cathode assemblies can be represented by equation (1): (metal oxide) + 2e- (reduced metal) + 02- (1) ddr 2e- of the current supplied by the cathode assembly 1300 .
[25] At the anode assembly 1200, negative oxygen ions charged in the electrolyte can transfer their negative charge to the anode assembly 1200 and be converted to oxygen. The electrolysis reaction at the anode assemblies can be represented by equation (2): 2- -> 02 + 4e- (2) ddr 4e- ãr the current passing into the anode assembly 1200.
[26] If, for example, a small Li-based salt is used as the electrolyte, the above cathode reaction can be reversed by equation (3): (metal oxide) + 2e- + 2Li + (metal oxide) + 2Li (reduced metal) + 2Li + + 02- (3) However, this specific reaction sequence need not occur, and intermediate electrode reactions are possible, as if cathode assembly 1300 is maintained at a less negative potential than that at which lithium deposition will occur. Possible intermediate electrode reactions include those represented by equations (4) and (5): (metal oxide) + xe- + 2Li + Lix (metal oxide) (4) Lix (metal oxide) + (2 - x) e- + (2 - x) Li + (reduced metal) + 2Li + +0215) Incorporation of lithium into the crystal structure of the metal oxide in the intermediate reactions shown in (4) and (5) can improve conductivity of the metal oxide, which promotes reduction.
[27] Reference electrodes and other chemical or electrical monitoring devices can be used to check the electrode potentials and reduction rate and thus the risk of anodes of cathode damage / corrosion / overheating, etc. For example, reference electrodes may be located near a cathode surface to monitor electrode potential and adjust electrode voltage. even potential sufficient only for reduction can avoid anode reactions such as chlorine evolution and cathode reactions such as free-flowing droplets of electrolyte metal such as lithium or calcium.
[28] [0028] Efficient transport of loose oxidation moieties in a liquid electrolyte, e.g. Li20 in narrow LiC1 used as electrolyte, can improve the rate of reduction and production of unoxidized metal in exemplary embodiment EORS 1000. Alternating anode assemblies 1200 and cathode assemblies 1300 can improve lost oxidation maturity and smoothness through the electrolyte, while increasing anode and cathode surface area for large scale anode. Exemplary Embodiment EORS 1000 may further include an 11 agitator, mixer, vibrator, or the like to enhance diffusion transport of the loose oxidation moieties.
[29] Chemical and / or electrical monitoring may indicate that the reduction process described above has been shortened in the end, such that a voltage potential between anode assembly 1200 and cathode assembly 1300 increases or an amount of loose oxidation ions is reduced. At a desired degree of completion, the reduced metal formed in the reduction process discussed above can be harvested from cathode assembly 1300, by lifting cathode assembly 1200 containing the remaining reduced metal out of the electrolyte in container 1050. Oxygen collected at the anode assemblies during process 1200 can be applied periodically or continuously. removed from the units and discharged or collected for further use.
[30] Although the structure and operation of the exemplary embodiment EORS 1000 has been shown and described above, it is understood that several different components described in the incorporated documents and elsewhere are useful with exemplary embodiments and may describe, in further detail, specific operations and features. of EORS 1000. In a similar manner, components and functionality of exemplary embodiment EORS 1000 are not limited to the specific details given above or in the incorporated documents, but may be varied as needed and by those skilled in the art.
[31] FIG. 3 is an illustration of an exemplary embodiment of modular anode assembly 200 usable with exemplary embodiment 12 EORS 1000. For example, modular anode assembly 200 may be used as anode assembly 1200 described above with reference to Fig. 1. Exemplary Embodiment of Modular Anode Assembly 200 may include systems and components using anodes.
[32] SA shown in Fig. 3, exemplary embodiment of modular anode assembly 200 includes one or more anode rods 210. Each anode rod 210 may extend down from a channel frame 201 for a sufficient distance to come into electrical contact with an electrolyte below the assembly 200. For example, when used in EORS 1000 (Fig. 1), an anode rod 210 will have a length greater than a distance from a bottom of anode assembly 1200 to a top level 1052 of the electrolyte in the electrolyte container 1050. Anode rods 210 may be evenly spaced or grouped along duct frame 201 of exemplary embodiment modular anode assembly 200, depending on which oxidation of oxidation ions is desired in an electrolytic oxide reduction system. For example, as shown in Fig. 3, four anode rods 210 may be evenly aligned along channel frame 201, so as to present an even current or charge distribution through an electrolyte when placed on each side of cathode assembly 1300 (Fig. 1). Furthermore, since cathode assemblies 1300 useful in exemplary embodiments EORS 1000 may be planar with increased volume to accommodate larger amounts of metal oxides, anode rods 210 lined substantially uniformly along channel frame 201 may remove oxidations uniformly from an electrolyte around the planar cathode assemblies 1300 and / or provide equal oxidation potentials to the same. An example of cathode assemblies that can be alternated with exemplary 13 modular salt anode assemblies is described in the incorporated document U.S. Pat. application number 12/978005, filed December 23, 2010.
[33] An anode rod can be made of a variety of conductive materials that retain their physical properties when exposed to electrolytic or oxidizing conditions and operating temperatures of several hundred degrees Celsius. For example, any corrosion-resistant metal alloy may be used in anode rod 210. In the example using a high temperature mixture of alkaline halide salt as electrolyte, a particular heat and corrosion-resistant material, such as platinum, may be used for a lower portion 211 of anode rod 210 which extends below electrolyte level_ 1052. Platinum, iridium, rhodium and their alloys, and other noble, conductive materials may equally be used for anode rod 210, or a lower part 211 thereof. Furthermore, sacrificial material, such as graphite, can be used for anode rod 210, or a bearing portion 211 thereof. Sacrificial material can react readily with oxygen developed at the anode and / or released from the electrolyte to form less reactive / corrosive gases, such as carbon dioxide.
[34] To reduce cost, an upper part 212 of anode rod 2 can be made of a richer material such as a nickel alloy which is electrically conductive and heat and corrosion resistant. That is, since the upper part 212 can not come into contact with reactive electrolyte, a cheap but comparatively resilient material can be used in the upper part 212, such as stainless steel or nickel, instead of a more unusual material such as platinum, iridium or rhodium. . Alternatively, or in addition, bearing portion 211 may be non-enlargeable removable upwardly portion 212 to allow 14 material differences between these sections and allow easy replacement and / or repair of bearing portion 211 due to, for example, corrosion or other damage. caused by high electrolyte operating temperature or electrolysis. The upper part 212 may be removably mated with the lower part 211 by any of several known assembly mechanisms such as mechanical fasteners, screws and threaded slides, pinheads and receivers, etc.
[35] One or more instrumentation guides 220 may further be housed in channel frame 201 or otherwise connected to exemplary embodiments of modular anode assembly 200. Instrumentation guides 220 may provide guidance for inserting individual assemblies 200 at fixed positions within a larger system, such as EORS 1000. for example, and can facilitate easy insertion and removal of exemplary embodiments of modular anode assembly 200 from smart systems based on need. Instrumentation controller 220 may also accommodate electrical and / or chemical sensors that monitor physical aspects of unit 200 and systems using the same to determine and control reduction potential and completeness. For example, chemical instrumentation supplying oxide ions in the electrolyte, or an electrode supplying current current in an anode rod 210 may be placed in instrumentation guides 220 and connected to an exterior output device or processor (not shown) to analyze system parameters and control their use.
[36] Duct frame 201 may include an electrical and / or thermally insulating member attached thereto to lower the operating temperature of duct frame 201 and adjacent components and to avoid current flow outside exemplary embodiment of anode assembly 200, such as into a larger EORS system 1000 (Figs. 1). For example, insulating member 202 may thank an entire bearing or outer surface of assembly 200, or may be positioned on channel frame 201 only where channel frame 201 should come into contact with an external stand, such as top plate 1108 or around knife wall contacts of busbar 280 (discussed below). ), or may be positioned ddr anode rods 210 connect to channel frame 201 shown in Fig. 3. Insulating member 202 may be made of a ceramic or fluorocarbon, such as polytetrafluoroethylene, or the like to provide thermal and / or electrical insulation.
[37] An anode guard 205 may further be joined to duct frame 201 and enclose electrical components of exemplary embodiment modular anode assembly 200. Anode guard 205 may insulate and / or prevent inadvertent contact with current-carrying assembly components while handling assembly 200. Anode shields may be electrically shielded. components and the like allow cooling mechanisms, such as a cooling gas line 240 and / or exhaust line 245 (described below) to extend frail and into the assembly 200. Anode protection 205 may be made of a material which is insulating and resistant to oxygen corrosion and / or elevated temperatures; such material may be a solid plate or may be a ndt which allows gases and heat to flow outside the unit 200. A lifting bag 290 or other handling mechanism may be assembled to the anode guard 205 or other component of the unit 200 to assist in handling / insertion / removal of exemplary embodiment modular anode assemblies 200. In this manner, channel frame 201, anode guard 205 and lift bag 290 may provide insulating and secure operating conditions and 16 handling mechanisms for easily moving, inserting or removing exemplary embodiments modulating anode assemblies to systems for systems, as EORS 1000 (Fig. 1).
[38] FIG. 4 is another illustration of an exemplary embodiment of anode assembly 200 with anode guard 205 or lift bag 290, showing electrical and cooling internal components usable therein. As shown in Fig. 4, anode rods 210 and / or instrumentation guides 220 may be located in channel frame 201 through holders 215. HAHare 215 may securely and removably join channel frame 201 and anode rod 210 so as to provide anode rods 210 there insulating from channel frame 201. For example, holder 215 may be a ceramic sleeve, nut or screw, a bolt having an insulating liner, etc.
[39] Anode rod 210, regardless of its position or orientation within assembly 200, electrically driven by an electrical system of exemplary embodiment modular anode assembly 200. For example, an electrical system may include an anode block 286, slider 285 and sampling rail 280, which provide current and / or voltage to one or more anode rods 210. In the example shown in Fig. 4, anode rod 210 or an is placed into an insert or slide in anode block 286 to maximize surface area contact between anode block 286 and anode rod 210. Electrically connected anode block 286 through lateral contacts at a slide contact 285 to busbar 280. Anode block 286, slide switch 285, and busbar 280 may each be insulated from and / or otherwise not electrically connected to channel frame 201 and anode guard 205 (Fig. 3). For example, the one shown in Fig. 4, dr slider 285, anode block 286, and busbar 280 are each raised from and separated from 17 channel frame 201. Where these elements come into contact with other charged components, such as anode rods 210 joining to anode block 286 at channel frame 201 or where knife wall contacts of busbar 280 extend through channel frame 201, an insulator may be provided between the contact and the channel frame 201.
[40] Sliding contact 285 allows thermal expansion of anode block 286 and / or busbar 280 without movement of anode rod 210 or resulting damage. That is, anode blocks 286 and / or busbars 280 can expand and / or converge transversely past each other in sliding contact 285, while still remaining in lateral electrical contact. Each component of the exemplary electrical system is made of electrically conductive materials, such as copper or iron alloys and the like. Any number of components may be repeated within the electrical system, for example, several anode blocks 286 may be positioned to connect to several corresponding anode rods 210 while still each connecting to a plurality of busbars 280 at either end of exemplary embodiment modular anode assembly 200. which can connect to corresponding synchronized voltage heads.
[41] An electrical system protected by anode guard 205 (Fig. 3) and isolated from duct frame 201 and anode guard 205 (Fig. 3) may be connected to an external electrical cold. For example, busbar 280 may include a knife wall connector extending through, and isolated from, channel frame 201. The knife wall connector of busbar 280 may be located in a knife wall receiver of EORS 1000 (Fig. 1) at defined positions where exemplary embodiments of modular anode assembly 200 18 may be placed. Independent electric current and / or voltage of desired levels may be provided to anode rod 210 through busbar 280, slider 285 and anode block 286, so that anode rods 210 may provide an oxidizing potential / oxygen deionizing function in a reducing system. Voltage and / or current provided by an electrical system in exemplary embodiment assembly 200 may be varied by an external controller, manual or automated, based on physical parameters of a system and circuit & Am instrumentation, which may also be provided by exemplary embodiment anode assembly 200. Alternatively For example, electrical systems in exemplary embodiments of modular anode assemblies may be free-standing and driven by internal high-capacity electrical bearings, without the need for external connectors.
[42] An exemplary embodiment of the modular anode assembly 200 may further include a cooling system that assists in maintaining electrical components and other assembly structures at an operating temperature that improves material stability, electrical conductivity, and safety. For example, apart from the lower part 211 (Fig. 3) of anode rods 210 which are in direct contact with possibly molten halide salts, an operating temperature of exemplary embodiment modulating anode assemblies 200 above top plate 1108 may be maintained at about 150 ° C or hover. Insulating part 202 can further contribute to a lower operating temperature.
[43] Refrigerant systems may comprise, for example, a cooling line 2 for active gas and a gas outlet line 245 connected and / or vented to exemplary embodiment modular unit 200. As shown in Fig. 4, lines 240 and 245 may enter unit 200 from one side or both 19 sides and extend along each anode block 286 within anode cover 205 (Fig. 3). Pipes 240 and 245 may connect to corresponding gas wells and drains included in or independently frail a modular system said. as EORS 1000 (Fig. 1). Gas outlet line 245 and cooling line 240 for active gas may be mutually or individually supported by line support 248 secured to duct frame 201 and insulated from an electrical system. Active gas cooling line 240 may include one or more drainage halls 241 which blow a refrigerant gas directly onto an anode block 286 or other component desired to be actively cooled. Since anode block 286 can connect to anode rod 210 in a higher temperature electrolyte, anode block 285 may be a hottest or most efficiently cooled component in an exemplary embodiment modular anode assembly 200. Further or alternatively, line 240 for active gas may ventilate or blow refrigerant gas onto a variety of structures and / or generally cooling an inside of anode cover 205 (Fig. 3). Of course, closed ducts and compressor / coolant-based cooling systems, or systems using multiple coolant lines 240, etc., can be looped by exemplary embodiment of modular anode assemblies and provide desired cooling.
[44] The active refrigerant gas may be a cooled, inert gas such as argon, helium etc. which convectively removes heat from the exemplary embodiment of modular anode assembly 200. The active refrigerant gas may further be mixed with oxygen or other exhaust gases left from the electrolyte or material to be reduced in reduction systems and can flood into or collect in exemplary embodiment anode assembly 200. The mixture can both cool and reduce the corrosivity of hot exhaust gases; for example, cooled neon mixed with hot, potentially ionized, gaseous oxygen will, by dilution, reduce the temperature and corrosivity of such oxygen without further reaction.
[45] Active refrigerant gas and any mixed exhaust gas can be swept into gas outlet line 245 for ventilation or further use. Gas outlet line 245 may have slides, ventilation slots, filters, etc. and be connected to an external Mkt or cooler which provides a relatively low pressure in gas outlet line 245, such that gases in exemplary embodiments anode assembly 200, especially coolant and exhaust gases collected under anode protection 205 (Fig. 3) will be swept into gas outlet line 245. Gas outlet line 245 may further include a sweep vent line 246 connected thereto. A sweep collecting and concentrating oxygen and / or other exhaust gases from a reduction system may connect to the exemplary embodiment anode assembly 200 and feed such gases directly into the gas outlet line 245 through the sweep vent line 246. The exhaust gases from such a sweep may mix and be cooled with the gas contained therein. into gas outlet line 245 for things handling and reduced corrosion. An example of a sweeping device assembling into an exemplary embodiment is described in the incorporated application U.S. application number 12/97779, filed December 23, 2010.
[46] Gas lines 240 and 245 may be simply and non-destructively connected and disconnected to respective coolant gas valves or pressure anchors ddr exemplary embodiment modular anode assembly 200 dr positioned in a reducing system, such as EORS 1000 (Fig. 1) or another system. For example, reducing systems may include a glove box tube which can connect, via a fastener, screw, rudder coupling, etc., to gas outlet line 245 and draw exhaust gas and spent refrigerant gas into the glove box for insulation and handling.
[47] The SA shown in Fig. 1 is an exemplary embodiment of modular anode assemblies 200 usable as anode assemblies 1200 and can be standardized and used in a replaceable combination, in numbers based on oxidation requirements. For example, if each modular anode assembly 200 includes, similarly configured, busbars 280 with knife wall connectors and outlets for gas lines 240 and 245, any modular anode assembly 200 may be replaced with another or moved to other correspondingly configured locations. within a reducing system, such as EORS 1000. Each anode assembly can be operated and placed in the vicinity, as rotated, with a cathode assembly to provide a desired and effective reduction action to metal oxides in the cathodes. Sas: In flexibility, the large amount of reduced metal can be formed in predictable, even amounts with controlled resource consumption and reduced system complexity and / or risk of damage in exemplary embodiments using exemplary embodiments modulating anode assemblies 200.
[48] Exemplary embodiments discussed above may be used in unique reduction processes and methods associated with exemplary systems and anode assembly embodiments. Exemplary methods include determining the position or configuration of one or more modular anode assemblies within a reduction system. Such determination may be based on an amount of material to be reduced, desired operating power levels or temperatures, cathode assembly positions, and / or any other set or desired operating parameter of the system. Exemplary methods can further connect anode units to a power source and an optional gas source / drain, such as a glove box where the units are located. Since exemplary assemblies are modular, external connections can also be uniform, and a single type of connection can work with all exemplary anode assemblies. An electrolyte used in reduction systems can be smolt or liquid to position anode and / or cathode assemblies at the designated positions in contact with the electrolyte.
[49] A desired power level, matte in either current or voltage, is provided to anode assemblies by an electrical system in the assemblies to thereby charge anode rods therein in exemplary methods. This charge reduces, while the anode rods are in contact with an electrolyte, a metal oxide in adjacent cathodes or in contact with the same in the electrolyte, while deionizing oxygen lost into the electrolyte. Exemplary methods may further replace modular parts of assemblies or entire assemblies within reduction systems based on the need for repair or system configuration, providing a flexible system that can produce varying amounts of reduced metal and / or be operated at desired power levels, electrolyte temperatures, and / or whichever preferably another system parameter based on modular configuration. After reduction, the reduced metal can be removed and used in a variety of chemical processes based on the identity of the reduced metal. For example, reduced uranium metal can be processed into nuclear fuel. 23
[50] Exemplary Methods Thus Described, It will be appreciated by those skilled in the art that exemplary embodiments may be varied by routine experimentation and without further inventive action. For example, although four anode rods are shown in exemplary embodiments, it is to be understood that other numbers and configurations of anode rods may be used based on expected anode assembly location, power level, required anodizing potential, etc. Variations should not be construed as deviating from the spirit or scope of the exemplifying embodiments. the embodiments, and all such modifications as would be apparent to those skilled in the art are intended to be included within the scope of the following claims. 24
权利要求:
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KR101292967B1|2013-08-02|DEVICE OF THE ADVANCED Cd| DISTILLATION
同族专利:
公开号 | 公开日
US8956524B2|2015-02-17|
GB201313053D0|2013-09-04|
KR101767712B1|2017-08-11|
US20120160704A1|2012-06-28|
CN103261491B|2016-04-20|
KR20140000288A|2014-01-02|
WO2012087399A1|2012-06-28|
GB2501041B|2016-11-02|
GB2501041A|2013-10-09|
JP2014501331A|2014-01-20|
SE1350853A1|2013-07-09|
FI20135785A|2013-07-19|
JP5849100B2|2016-01-27|
CN103261491A|2013-08-21|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US422139A|1890-02-25|Daniel m |
US658891A|1899-05-11|1900-10-02|S D Warren & Co|Electrode and electrode connection.|
GB284678A|1927-02-03|1928-11-29|Paul Leon Hulin|
US2089738A|1935-08-10|1937-08-10|Redler Conveyor Co|Conveyer|
US2194444A|1937-07-06|1940-03-19|Du Pont|Fused salt electrolysis cell|
GB506590A|1937-11-29|1939-05-30|George William Johnson|Improvements in the electrolytic manufacture and production of zinc dust|
US2766198A|1953-03-05|1956-10-09|Union Carbide & Carbon Corp|Anodes for electrowinning of manganese|
US2800219A|1954-09-30|1957-07-23|Ance E Carroll|Conveyor for handling pulverized uranium|
US2913380A|1957-06-20|1959-11-17|Chicago Dev Corp|Refining titanium-vanadium alloys|
US2967142A|1958-09-22|1961-01-03|Union Carbide Corp|Blade electrode assembly|
US3286136A|1963-09-20|1966-11-15|Bell Telephone Labor Inc|Fabrication of electrodes from modular units|
US3479225A|1966-03-15|1969-11-18|Leesona Corp|Oxygen depolarized electrochemical modular units|
US3531269A|1967-04-21|1970-09-29|Intern Steel Slag Corp|Molten steel slag handling process and apparatus|
US3562131A|1968-03-21|1971-02-09|Bunker Hill Co|Cathode handling equipment|
US3645708A|1969-12-04|1972-02-29|Int Steel Slag Corp|Steel slag handling system and method for using|
US3697404A|1971-01-29|1972-10-10|Peter M Paige|Apparatus to support the electrodes and bus bars in an electrolytic cell|
BE791042A|1971-11-09|1973-03-01|Oronzio De Nora Impianti|BIPOLAR ELECTROLYSIS CELL|
AU498239B2|1973-09-26|1979-02-22|Lamm, August Uno.|A chlorinator cell|
GB1476055A|1975-03-05|1977-06-10|Imp Metal Ind Kynoch Ltd|Eletro-winning metals|
US4025400A|1975-08-11|1977-05-24|Duval Corporation|Process and apparatus for the recovery of particulate crystalline product from an electrolysis system|
DE2600344A1|1976-01-07|1977-07-14|H T Hydrotechnik Gmbh|Water electrolyser cell stack - using thin walled channel frame with web strips supporting channel flanges|
US4023673A|1976-01-22|1977-05-17|Veda, Inc.|Conveyor drop structure|
US4013329A|1976-02-23|1977-03-22|Multilam Corporation|Multiple plate assembly for forming electrical connector or switch|
US4073703A|1976-12-14|1978-02-14|Aluminum Company Of America|Electrolytic production of magnesium|
DE2728634C2|1977-06-24|1979-03-08|Siemens Ag, 1000 Berlin Und 8000 Muenchen|Ultrasonic solder bath with a sonotrode arranged with a solder bath container|
US4148392A|1977-07-11|1979-04-10|Prab Conveyors, Inc.|Viscid material conveyor|
CA1142123A|1980-01-31|1983-03-01|Hugh D. Kelley|Conveyor for handling free-flowing material|
DE3005795C2|1980-02-15|1984-12-06|Conradty GmbH & Co Metallelektroden KG, 8505 Röthenbach|Coated metal anode for the electrolytic extraction of metals|
US4437968A|1980-09-10|1984-03-20|Zerpol Corporation|Boiler apparatus|
US4326937A|1980-09-16|1982-04-27|Par Systems Corp.|Grab mechanism|
IT1157026B|1982-06-04|1987-02-11|Ginatta Marco Elettrochim|METHOD FOR THE ELECTROLYTIC LEAD PRODUCTION|
US4492621A|1982-09-29|1985-01-08|Stubb Paul R|Method and apparatus for electrodeposition of materials|
US4668353A|1984-10-10|1987-05-26|Desom Engineered Systems Limited|Method and apparatus for acid mist reduction|
JPS60194090A|1984-03-16|1985-10-02|Mitsubishi Chem Ind Ltd|Electrolytic cell for titanium|
US4608135A|1985-04-22|1986-08-26|Aluminum Company Of America|Hall cell|
EP0286092B1|1987-04-10|1993-01-07|Mitsubishi Materials Corporation|Apparatus for hanging and handling plate members|
CN87207164U|1987-06-10|1988-12-07|周昌明|Stereoscopic platinum anode electrolytic tank|
US4880506A|1987-11-05|1989-11-14|The United States Of America As Represented By The Department Of Energy|Electrorefining process and apparatus for recovery of uranium and a mixture of uranium and plutonium from spent fuels|
NO162975C|1987-12-30|1990-03-14|Norsk Hydro As|PROCEDURE FOR SETTING ELECTRODES IN ELECTROLYCLE CELLS.|
US4936971A|1988-03-31|1990-06-26|Eltech Systems Corporation|Massive anode as a mosaic of modular anodes|
IT1219222B|1988-04-19|1990-05-03|Ginatta Spa|PROCEDURE FOR THE ELECTROLYTIC PRODUCTION OF A MULTI-PURPOSE METAL AND EQUIPMENT FOR THE IMPLEMENTATION OF THE PROCEDURE|
US4863580A|1988-08-10|1989-09-05|Epner R L|Waste metal extraction apparatus|
US4946026A|1989-08-28|1990-08-07|Ogden Environmental Services, Inc.|Residue removal system for a conveyor assembly|
CN2101839U|1991-04-24|1992-04-15|冶金工业部鞍山热能研究院|Anode with forced cooling ac arc furnace bottom|
US5279715A|1991-09-17|1994-01-18|Aluminum Company Of America|Process and apparatus for low temperature electrolysis of oxides|
JP3074919B2|1992-03-31|2000-08-07|三菱マテリアル株式会社|Cathode scraper driving device in electrolytic cell|
US5454914A|1993-12-23|1995-10-03|The United States Of America As Represented By The United States Department Of Energy|Method of removal of heavy metal from molten salt in IFR fuel pyroprocessing|
US5531868A|1994-07-06|1996-07-02|The United States Of America As Represented By The United States Department Of Energy|Advanced electrorefiner design|
DE29505938U1|1995-04-06|1996-08-08|Stocko Metallwarenfab Henkels|Electrical contact element and plastic housing for receiving the contact element|
US5935394A|1995-04-21|1999-08-10|Alcan International Limited|Multi-polar cell for the recovery of a metal by electrolysis of a molten electrolyte|
US5582706A|1995-06-02|1996-12-10|Rockwell International Corporation|Electroseparation of actinide and rare earth metals|
US5770034A|1995-07-15|1998-06-23|Agfa-Gevaert N.V.|Process and apparatus for desilvering a silver-containing solution|
JPH0972991A|1995-09-05|1997-03-18|Ishikawajima Harima Heavy Ind Co Ltd|Method and device for electrolytic separation for actinoid element and lanthanoid element|
FR2738661B1|1995-09-11|1997-11-28|Framatome Sa|DEVICE AND METHOD FOR RECOVERING AND COOLING THE FUSED HEART OF A NUCLEAR REACTOR|
US5855749A|1997-05-29|1999-01-05|Electrocopper Products Limited|Ventilation system for electrolytic cell|
DE19845258C1|1998-10-01|2000-03-16|Hamburger Aluminium Werk Gmbh|Installation for sucking away waste gases and using their heat for aluminum multi cell electrolysis plant comprises waste gas collector hoods and suction ducts for each electrolysis cell of the plant|
US6142291A|1998-12-31|2000-11-07|Sidney Manufacturing Company|Self-cleaning inclined section for drag conveyor|
FI107941B|1999-06-10|2001-10-31|Outokumpu Oy|Apparatus for transferring electrodes in electrolytic refining of metals|
NO20010927D0|2001-02-23|2001-02-23|Norsk Hydro As|Method and apparatus for making metal|
WO2002072939A2|2001-03-13|2002-09-19|Unilever N.V.|Reciprocating washing machine.|
US6827828B2|2001-03-29|2004-12-07|Honeywell International Inc.|Mixed metal materials|
US6689260B1|2001-08-29|2004-02-10|The United States Of America As Represented By The United States Department Of Energy|Nuclear fuel electrorefiner|
US6540902B1|2001-09-05|2003-04-01|The United States Of America As Represented By The United States Department Of Energy|Direct electrochemical reduction of metal-oxides|
US6866768B2|2002-07-16|2005-03-15|Donald R Bradford|Electrolytic cell for production of aluminum from alumina|
NO318164B1|2002-08-23|2005-02-07|Norsk Hydro As|Method for electrolytic production of aluminum metal from an electrolyte and use of the same.|
US6911134B2|2002-09-06|2005-06-28|The University Of Chicago|Three-electrode metal oxide reduction cell|
JP2004115889A|2002-09-27|2004-04-15|Dowa Mining Co Ltd|Cooling device for electrode used in electrolytic smelting|
WO2004031453A1|2002-10-04|2004-04-15|Michael John Sole|Electowinning of metals|
AU2002952181A0|2002-10-21|2002-11-07|Intec Ltd|Electrolysis process and cell for use in same|
AU2002952743A0|2002-11-19|2002-12-05|Waterpower Systems Pty Ltd|Electrocoagulation system|
US20040134785A1|2003-01-09|2004-07-15|The University Of Chicago|Advanced high-throughput electrorefiner design|
TWI322198B|2003-01-22|2010-03-21|Toyo Tanso Co|Electrolytic apparatus for molten salt|
KR100593790B1|2003-03-28|2006-07-03|한국원자력연구소|Method for electrolytic reduction of oxide spent fuel in LiCl-Li2O, cathode electrode assembly for applying the method, and device having the cathode electrode|
US7097747B1|2003-08-05|2006-08-29|Herceg Joseph E|Continuous process electrorefiner|
US7011736B1|2003-08-05|2006-03-14|The United States Of America As Represented By The United States Department Of Energy|U+4 generation in HTER|
JP3913725B2|2003-09-30|2007-05-09|日鉱金属株式会社|High purity electrolytic copper and manufacturing method thereof|
WO2005035404A1|2003-10-14|2005-04-21|Raijmakers Leon Fatima Peter H|Scraper conveyor|
US7267754B1|2004-01-21|2007-09-11|U.S. Department Of Energy|Porous membrane electrochemical cell for uranium and transuranic recovery from molten salt electrolyte|
DE102004018554B4|2004-04-14|2018-09-27|Wago Verwaltungsgesellschaft Mbh|Jumper for electrical terminals|
WO2006007863A1|2004-07-16|2006-01-26|Cathingots Limited|Electrolysis apparatus with solid electrolyte electrodes|
JP2006083466A|2004-08-17|2006-03-30|Furukawa Electric Co Ltd:The|Apparatus for recovering metal|
JP2006129439A|2004-09-28|2006-05-18|Kyocera Corp|Communication system, base station apparatus, server apparatus, mobile station apparatus, and transmission data amount determining method|
DE202004018757U1|2004-12-04|2006-04-13|Weidmüller Interface GmbH & Co. KG|Device for the electrical bridging of two busbars|
CN101155947B|2005-03-24|2010-09-08|Bhp比利顿创新公司|Anode support apparatus|
JP4504247B2|2005-04-28|2010-07-14|株式会社東芝|Minor actinide recycling method|
US7638026B1|2005-08-24|2009-12-29|The United States Of America As Represented By The United States Department Of Energy|Uranium dioxide electrolysis|
US7449635B2|2006-03-06|2008-11-11|Siemens Energy & Automation, Inc.|Bus joint assembly|
US7563982B2|2006-11-30|2009-07-21|Continental Automotive Systems Us, Inc.|Bus bar assembly|
DE102006062206B4|2006-12-22|2011-06-16|Minebea Co., Ltd.|Fluid dynamic bearing with axial preload|
US7744734B2|2007-08-24|2010-06-29|Battelle Energy Alliance, Llc|High current density cathode for electrorefining in molten electrolyte|
US7993501B2|2007-11-07|2011-08-09|Freeport-Mcmoran Corporation|Double contact bar insulator assembly for electrowinning of a metal and methods of use thereof|
CN101453071B|2007-11-28|2013-05-08|李世煌|Conductive body for electric power plug, socket and socket connector with conductive material improved|
US8097142B2|2008-02-29|2012-01-17|Uchicago Argonne, Llc.|High-throughput electrorefiner for recovery of U and U/TRU product from spent fuel|
WO2009122705A1|2008-03-31|2009-10-08|株式会社キノテック・ソーラーエナジー|Electrolysis vessel|
WO2010080761A1|2009-01-06|2010-07-15|Epner R L|System for electrolytic recovery of metals with improved connection interface|
US7980384B2|2009-04-30|2011-07-19|Hapman, Inc.|Tensioning device for drag conveyor|
US20110100328A1|2009-10-29|2011-05-05|Prime Core Tech LLC.|Electrolysis apparatus and related devices and methods|
US8248760B2|2010-07-07|2012-08-21|Eaton Corporation|Switch arrangement for an electrical switchgear|
US9777910B2|2015-03-24|2017-10-03|Atlas Lighting Products, Inc.|LED based area lighting fixture|US10221499B2|2015-06-25|2019-03-05|Ge-Hitachi Nuclear Energy Americas Llc|Nuclear fuel structure and method of making a nuclear fuel structure using a detachable cathode material|
TWI649458B|2017-11-22|2019-02-01|財團法人工業技術研究院|Plating apparatus|
US10872705B2|2018-02-01|2020-12-22|Battelle Energy Alliance, Llc|Electrochemical cells for direct oxide reduction, and related methods|
GB2570700A|2018-02-03|2019-08-07|Richard Scott Ian|Continuous processing of spent nuclear fuel|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
US12/977,916|US8956524B2|2010-12-23|2010-12-23|Modular anode assemblies and methods of using the same for electrochemical reduction|
PCT/US2011/053872|WO2012087399A1|2010-12-23|2011-09-29|Modular anode assemblies and methods of using the same for electrochemical reduction|
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